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Assessment of an alternative meropenem dosing strategy compared with imipenem-cilastatin or traditional meropenem dosing after cefepime failure or intolerance in adults with neutropenic fever.

AbstractSTUDY OBJECTIVE:
To compare clinical outcomes of patients receiving an alternative dosage of meropenem with those of patients receiving imipenem-cilastatin or the traditional dosage of meropenem after failure of or intolerance to cefepime for treatment of febrile neutropenia.
DESIGN:
Retrospective, single-center cohort study.
SETTING:
1250-bed urban academic medical center.
PATIENTS:
One hundred twenty-seven adults with neutropenic fever who received either imipenem-cilastatin or meropenem; imipenem-cilastatin was the preferred carbapenem until September 1, 2006, after which meropenem became the formulary carbapenem.
MEASUREMENTS AND MAIN RESULTS:
Of the 127 patients, 40 received imipenem-cilastatin 500 mg every 6 hours between September 1, 2005, and August 31, 2006; 87 patients received meropenem between September 1, 2006, and August 31, 2007: 29 received a traditional dosage of meropenem 1 g every 8 hours, and 58 received an alternative dosage of meropenem 500 mg every 6 hours. Primary outcomes of time to defervescence (median 3 vs 2 vs 3 days), need for additional antibiotics (20% vs 17% vs 14%), and time to receipt of additional antibiotics (median 5 vs 2 vs 1 days) were not significantly different among the imipenem-cilastatin, traditionally dosed meropenem, and alternatively dosed meropenem groups, respectively. In addition, significant differences in secondary outcomes, which were treatment duration (median 10 vs 8 vs 8 days), seizure rate (0% vs 0% vs 0%), in-hospital mortality (5% vs 7% vs 7%), and 30-day mortality (13% vs 7% vs 14%), were not identified among the three groups, respectively.
CONCLUSION:
The alternative meropenem dosage of 500 mg every 6 hours yielded similar patient outcomes, including time to defervescence, need for additional antibiotics, duration of therapy, and mortality, when compared with the traditional meropenem dosage and imipenem-cilastatin in adults with febrile neutropenia. In addition, no adverse effects on clinical outcomes were observed with the alternative dosage of meropenem.
AuthorsHeather M Arnold, Peggy S McKinnon, Kristan M Augustin, Lindsay M Hladnik, Ed Casabar, Richard M Reichley, Erik R Dubberke, Peter Westervelt, David J Ritchie
JournalPharmacotherapy (Pharmacotherapy) Vol. 29 Issue 8 Pg. 914-23 (Aug 2009) ISSN: 1875-9114 [Electronic] United States
PMID19637944 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • Anti-Bacterial Agents
  • Cephalosporins
  • Drug Combinations
  • Thienamycins
  • Cilastatin
  • Imipenem
  • Cefepime
  • Cilastatin, Imipenem Drug Combination
  • Meropenem
Topics
  • Adult
  • Anti-Bacterial Agents (administration & dosage, adverse effects)
  • Cefepime
  • Cephalosporins (adverse effects, therapeutic use)
  • Cilastatin (administration & dosage)
  • Cilastatin, Imipenem Drug Combination
  • Cohort Studies
  • Dose-Response Relationship, Drug
  • Drug Combinations
  • Female
  • Fever (complications, drug therapy, mortality)
  • Hospital Mortality
  • Humans
  • Imipenem (administration & dosage)
  • Male
  • Meropenem
  • Middle Aged
  • Neutropenia (complications, drug therapy, mortality)
  • Retreatment
  • Seizures (drug therapy)
  • Thienamycins (administration & dosage)
  • Time Factors

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